Perram J W, Reimann B, Klenk H D, Nicolau C, Polansky O E
Biophys Struct Mech. 1979 Mar 21;5(1):25-32. doi: 10.1007/BF00535770.
A kinetic model was constructed and partly solved to describe the migration of the fluorescence label 1,6-diphenylhexatriene (DPH) in both directions when enveloped viruses, labelled with DPH in their envelopes are in contact with unlabelled cells or cell labelled in their membranes are in contact with unlabelled enveloped viruses. The central assumption is that two types of receptor sites exist on the cell surface, i.e., physical adsorption sites (P-sites), available to all the viruses studied in these papers and binding sites (B-sites) available only to the viruses which penetrate into the specific cells. The differential equations for the label migration, for different values of the ratio number of viruses number of sites were numerically solved, assuming different fractions of P- and B-sites. The equations also describe, appropriately the mechanism of rapid label migration in the system and substantiate the magnitude "time of residence" of the nonpenetrating viruses adsorbed on the cell surface. The resulting curves match satisfactorily those for the label release by the viruses and account well for the steady state values of the kinetics of label migration in the virus-cell system.
构建并部分求解了一个动力学模型,以描述当包膜病毒在其包膜中用荧光标记物1,6 - 二苯基己三烯(DPH)标记后与未标记的细胞接触,或者细胞膜上标记有DPH的细胞与未标记的包膜病毒接触时,荧光标记物在两个方向上的迁移情况。核心假设是细胞表面存在两种类型的受体位点,即物理吸附位点(P位点),这些论文中研究的所有病毒都可利用该位点,以及仅对能够穿透特定细胞的病毒可用的结合位点(B位点)。对于不同的病毒数与位点数之比,在假设P位点和B位点的不同比例的情况下,对标记迁移的微分方程进行了数值求解。这些方程还恰当地描述了系统中标记快速迁移的机制,并证实了吸附在细胞表面的非穿透性病毒的“停留时间”大小。所得曲线与病毒释放标记物的曲线令人满意地匹配,并很好地解释了病毒 - 细胞系统中标记迁移动力学的稳态值。